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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Andrew R. Zinn

McDermott Center for Human Growth and Development

The University of Texas Southwestern Medical Center

Dallas

Texas 75390

USA

[email]@utsouthwestern.edu

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Affiliation

McDermott Center for Human Growth and Development, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA. 2002 - 2009

References

MODY-like diabetes associated with an apparently balanced translocation: possible involvement of MPP7 gene and cell polarity in the pathogenesis of diabetes. Bhoj, E.J., Romeo, S., Baroni, M.G., Bartov, G., Schultz, R.A., Zinn, A.R. Mol. Cytogenet (2009) [Pubmed]
EFHC2 SNP rs7055196 is not associated with fear recognition in 45,X Turner syndrome. Zinn, A.R., Kushner, H., Ross, J.L. Am. J. Med. Genet. B Neuropsychiatr. Genet. (2008) [Pubmed]
A Turner syndrome neurocognitive phenotype maps to Xp22.3. Zinn, A.R., Roeltgen, D., Stefanatos, G., Ramos, P., Elder, F.F., Kushner, H., Kowal, K., Ross, J.L. Behav. Brain. Funct (2007) [Pubmed]
Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndrome. Zinn, A.R., Ramos, P., Elder, F.F., Kowal, K., Samango-Sprouse, C., Ross, J.L. J. Clin. Endocrinol. Metab. (2005) [Pubmed]
Complete SHOX deficiency causes Langer mesomelic dysplasia. Zinn, A.R., Wei, F., Zhang, L., Elder, F.F., Scott, C.I., Marttila, P., Ross, J.L. Am. J. Med. Genet. (2002) [Pubmed]